Title of article :
A simplified Protocol to Induce Callogenesis in Protoplasts of Date Palm (Phoenix dactylifera L.) Cultivars
Author/Authors :
-، - نويسنده National Institute of Agronomic Resaerch of Algeria, Algeria Titouh, Kheyreddine , -، - نويسنده Department of Plant Production, LRGB- National School of Agronomy (ENSA), Algeria Khelifi, Lakhdar , -، - نويسنده Department of Plant Production, LRGB- National School of Agronomy (ENSA), Algeria Slaoui, Majda , -، - نويسنده National Institute of Agronomic Resaerch of Algeria, Algeria Boufis, Nazim , -، - نويسنده Department of Plant Production, LRGB- National School of Agronomy (ENSA), Algeria Morsli, Abdelkader , -، - نويسنده Department of Plant Production, LRGB- National School of Agronomy (ENSA), Algeria Hadj Moussa, Khadidja , -، - نويسنده Department of Biology, University of Western Ontario, London, ON Canada Makhzoum, Abdullah
Issue Information :
فصلنامه با شماره پیاپی 49 سال 2015
Pages :
10
From page :
26
To page :
35
Abstract :
-
Abstract :
Background: In Algeria, date palm is currently confronted to the Bayoud disease. Biotechnological tools such as protoplasts fusion can appear as an alternative to ensure rapid multiplication and improvement of this species.Objectives: Callogenesis induction in protoplasts isolated from embryogenic callus of three date palm cultivars.Materials and Methods: Some factors influencing the isolation and culture of protoplasts segregated from the calli of three date palm (Phoenix dactylifera L.) cultivars (Deglet Nour, Akerbouch and Degla Beida) were studied. Protoplasts of each cultivar were cultured on a semi-solid medium supplemented with various hormonal balances.Results: Maceration with an enzymatic solution containing 1.5% cellulase and 1% macerozyme R10 in the presence of 0.5 M mannitol for more than 16 h with gentle agitation allows isolation of a great number of viable protoplasts. In addition, purification of protoplasts on a cushion of 21 or 25% sucrose was effective in cell debris removal and maximum recovery. The culture of isolated protoplasts on a semi-solidified Murashige and Skoog medium, with 0.3% agarose, 2 mg. L-1 2,4-D and 0.5 mg.L-1 BAP allowed good viable protoplast maintenance as well as cell wall regeneration. After more than two months of culture, cell divisions were still occurring and microcalli became visible to the naked eye, containing a large number of cells.Conclusions: The developed protocol can be useful for application of somatic hybridization to improve date palm cultivars.
Journal title :
Iranian Journal of Biotechnology (IJB)
Serial Year :
2015
Journal title :
Iranian Journal of Biotechnology (IJB)
Record number :
2331900
Link To Document :
بازگشت